Evidence map›Paper›PMID 42833860›Full record

ArticleJournal for immunotherapy of cancer2026

Poliosis predicts durable response to immune-checkpoint blockade in metastatic melanoma: a multicenter cohort study.

Annika Brekner, Miriam Mengoni, Julian Kött, Berenice Mareen Lang, Alisa Lepper, Jakob Veeser, Janina Dietzel, Nora Laubach, Andrea Forschner, Christoffer Gebhardt and 3 more

Abstract readMulticenter Study
In one paragraph

Article in Journal for immunotherapy of cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Annika BreknerDepartment of Dermatology, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.
Miriam MengoniDepartment of Dermatology, Universitatsklinikum Schleswig-Holstein Campus Lubeck, Lübeck, Germany.
Julian KöttDermatology and Venereology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID http://orcid.org/0000-0003-2073-3909
Berenice Mareen LangDepartment of Dermatology, University Medical Center of the Goethe University Frankfurt, Frankfurt, Germany.
Alisa LepperDepartment of Dermatology, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.
Jakob VeeserDepartment of Dermatology, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.
Janina DietzelDepartment of Dermatology, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.
Nora LaubachDepartment of Dermatology, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.
Andrea ForschnerDepartment of Dermatology, University Hospital Tübingen, Tubingen, Germany.ORCID http://orcid.org/0000-0002-6185-4945
Christoffer GebhardtDermatology and Venereology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID http://orcid.org/0000-0001-7090-9584
Stephan Grabbe *Department of Dermatology, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.
Henner Stege *Department of Dermatology, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.
Maximilian Haist *Department of Dermatology, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany mhaist@stanford.edu.ORCID http://orcid.org/0000-0002-6720-7570

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmune checkpoint blockade (ICB) improved survival outcomes for patients with metastatic melanoma. Yet up to 65% of patients experience primary resistance and nearly half of initial responders acquire resistance. The clinical utility of ICB is further tempered by frequent immune-related adverse events (irAEs), which increase in severity and frequency with prolonged treatment duration. Hence, a pivotal challenge is to identify clinically accessible markers to predict durable ICB responses. While prior reports indicate that the development of cutaneous irAEs may reflect robust antitumor immune responses, there is limited evidence linking specific types of cutaneous irAEs to clinical ICB benefit.

methodsIn this retrospective multicenter study, we investigated a cohort of 741 patients diagnosed with non-resectable stage III/IV melanoma who were treated with ICB between April 2012 and August 2025. Patient demographics, tumor characteristics, treatment regimens and survival outcomes were collected within six German skin cancer centers. We stratified patients by the type of cutaneous AE into such with whitening of the body skin (vitiligo), hair (poliosis) or other cutaneous AE. Primary endpoints included progression-free survival (PFS) and objective response rates (ORR).

resultsAmong 741 eligible patients, 221 developed cutaneous irAE within the median follow-up period of 48 months. Thereof, we observed tumor recurrences in 17.2% of patients with poliosis, 57.7% of patients developing vitiligo and 60.0% of patients with other cutaneous irAE. In line, we detected a significantly enhanced ORR (93.1% vs 58.8% vs 38.8%, p

conclusionsOur study identifies poliosis as a distinct and immunologically-informed marker linked to strong and durable ICB responses easily applicable in a routine clinical setting. Detection of poliosis may complement radiographic imaging for clinical decision-making on ICB treatment duration and early cessation and provides a window for translational investigations harnessing epitope-specific T-cell responses to melanoma antigens.

Indexed as

Immune Checkpoint InhibitorsMelanomaSkin NeoplasmsAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedRetrospective StudiesImmune Checkpoint InhibitorsBiomarkerImmune Checkpoint InhibitorImmune related adverse event - irAEMelanoma

Identifiers

PMID42833860
PMCPMC13647029

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.